Digimed Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Digimed Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DHX-70H, XTG-70H, Hybrid C70, HYBRID S70
4
Total
4
Cleared
0
Denied
Digimed Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2023. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Digimed Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Innoden, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Digimed Co., Ltd.
4 devices